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• W2094720384 abstract "Fragile X mental retardation 1 gene (FMR1) expression is associated with fragile X syndrome (FXS) and exhibits several splicing products. However, the proportion of spliced isoforms that are expressed in different tissues remains unclear. In the present study, long‑chain reverse transcription‑polymerase chain reaction with a T cloning‑sequencing method was conducted in order to analyze the entire coding region of the FMR1 gene in human tissues. In particular, FXS‑associated tissues were analyzed, including the brain and testis. Twenty alternatively spliced isoforms were observed among 271 recombinants, including six novel ones. The isoform that consisted of the entire FMR1 coding region (ISO1) accounted for a small proportion of all isoforms. Isoforms lacking exon 12 were the most abundant. In particular, spliced isoforms ISO7 and ISO17 were the most abundant. However, their relative abundance varied between the peripheral blood cells, and the testis and brain tissues. Bioinformatic analyses suggested that exon 12 may be the sole exon undergoing positive selection. The results of the present study suggested that the mechanisms underlying alternative splicing (AS) of the FMR1 gene may be more complex. Furthermore, the functions of alternatively spliced products lacking exon 12 require further investigation. The results of the present study provide novel insights into the association between AS and the structure and function of the FMR1 gene." @default.
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• W2094720384 date "2015-03-31" @default.
• W2094720384 modified "2023-09-27" @default.
• W2094720384 title "Alternatively spliced products lacking exon 12 dominate the expression of fragile X mental retardation 1 gene in human tissues" @default.
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• W2094720384 doi "https://doi.org/10.3892/mmr.2015.3574" @default.
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